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SNOMED CT, US Edition
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/SNOMEDCT/5967006
http://purl.bioontology.org/ontology/SNOMEDCT/5967006
|
|---|---|
| Preferred Name | A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis |
| Synonyms |
A gamma beta<sup>+</sup> hereditary persistence of fetal hemoglobin AND beta<sup>0</sup> thalassemia in cis
A<sub>gamma</sub> beta<sup>+</sup> HPFH AND beta<sup>0</sup> thalassaemia in cis
A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis
A gamma beta+ hereditary persistence of fetal hemoglobin AND beta0 thalassemia in cis
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder)
A<sub>gamma</sub> beta<sup>+</sup> HPFH AND beta<sup>0</sup> thalassemia in cis
A gamma beta+ HPFH AND beta0 thalassemia in cis
A gamma beta+ HPFH AND beta0 thalassaemia in cis
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis
A gamma beta<sup>+</sup> hereditary persistence of fetal hemoglobin AND beta<sup>0</sup> thalassemia in cis (disorder)
A gamma beta+ hereditary persistence of fetal hemoglobin AND beta0 thalassemia in cis (disorder)
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | A gamma beta<sup>+</sup> hereditary persistence of fetal hemoglobin AND beta<sup>0</sup> thalassemia in cis
A<sub>gamma</sub> beta<sup>+</sup> HPFH AND beta<sup>0</sup> thalassaemia in cis
A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis
A gamma beta+ hereditary persistence of fetal hemoglobin AND beta0 thalassemia in cis
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder)
A<sub>gamma</sub> beta<sup>+</sup> HPFH AND beta<sup>0</sup> thalassemia in cis
A gamma beta+ HPFH AND beta0 thalassemia in cis
A gamma beta+ HPFH AND beta0 thalassaemia in cis
A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis
A gamma beta<sup>+</sup> hereditary persistence of fetal hemoglobin AND beta<sup>0</sup> thalassemia in cis (disorder)
A gamma beta+ hereditary persistence of fetal hemoglobin AND beta0 thalassemia in cis (disorder)
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|
|---|---|
| prefLabel | A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis
|
| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID |
900000000000020002
900000000000017005
|
| notation | 5967006
|
| Effective time | 20020131
|
| Active | 1
|
| Has finding site | |
| interprets | |
| subClassOf | |
| Semantic type UMLS property | |
| Has interpretation | |
| type | |
| Subset member |
447562003~MAPRULE~TRUE
6011000124106~MAPTARGET~D56.1
6011000124106~MAPADVICE~ALWAYS D56.4
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPTARGET~D56.4
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
900000000000497000~MAPTARGET~XUHEN
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPADVICE~ALWAYS D56.1
447562003~MAPTARGET~D56.4
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
447562003~MAPADVICE~ALWAYS D56.4
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
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| DEFINITION STATUS ID | 900000000000074008
|
| tui | T047
|
| CTV3ID | XUHEN
|
| Occurs in | |
| cui | C0271989
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| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |